Bone mets - please join in

[Magick]

Thank you all 🍀🍀🍀,
My mum was diagnosed with breat cancer T2N1aMo august 2013, ER,PR positiv, small Ki 12%. Trated neo chemo doxirubicin, partial brest save operation, after paklitaxel weekly( maybe it was before operation ) after radio therapy 28+5. She manage all well and kept working the same days of chemo was given. Than our life combeck to normal.
She had mammo control 12.11 and lung scan all was clean. But doctor start to be worried about slight higher level of suger in blood ( diabetes was not confirm ) , CAE 2,3 and CA 15-3was 35. Something start our super doctor bothered. Call my mum again for blood and CAE 2,8 and CA 15-3 was 51,9. And she start to do anything and everything ( so happy for such doctor ). All available scans, all clean, she discovered something in one survical vertebra C3 on PET/CT. Tomorrow early we go see our doctor. Mum has no pain, no deep breath and she is in very good shape. She celebrate 66 years 5.12.2018. I am not that crazy about researching internet ( i have done already enough, but only to be able to answer question of my mum as that made her somehow strong and she had none psycho fall down, she never asked the life prognosis ). And i found this forum. I thought it would be great co compare how it is treated elswhere, also shown other side ( daughters managing mother illness ) and having someone on side to understand.

[Pippin]

Hi Magick

You are welcome to join this site. Sorry to hear your mum has cancer. I got my first cancer diagnosis in August 2013 too. When my mum had breast cancer I wish there had been a site like this: I would have joined it. We are a "mixed bunch" meaning we are quite diverse. We can rant, learn to understand different points of view, sometimes even laugh and it certainly helps me to cope a little better sometimes. The site has been a bit quiet recently but there are a lot of people on it. Hundreds of years of experience I guess!

Pippin

[funnyface]

 Magick, I'm from the USA and I belong! Also we have had family members join before. How long has your mom had secondaries? Where did it come back at? Mine came back in my lungs 13 years ago. Welcome! FF

[Magick]

Lovely good evening ,
May i join your forum although i am from czech republik and not me, but my mother is cancer fighter since august 2013?

[Anne30]

Yes. I felt like that. Gradually you will get used to the treatment plan. I’ve been at this since March and now don’t think about it all the time. I hope you feel better soon x

[angiepops]

Hi anne30

Thanks for getting back to me, feeling very alone at the moment, like i m in a bubble.

Angie x

[gmc]

Sorry not to have replied earlier Riversidedawn - I thought I had already but obviously not .....which is another thing I'll put down to chemo brain..again ! I don't appear so far to have had any SE from the denosumab . The everolimus and exermestane are the tough ones for me. Even the BC nurse said they can be hard to tolerate but I was crying at the time so maybe she was just being kind to me !. After a scan 2 weeks ago they discovered pneuminitis in my lungs so have had a 2 week break to clear it up as caused by the treatment. Now I'm back on it at a reduced rate and so far so good....although worried that it will only be half as effective now!

Good wishes to everyone on this thread, Gill x

[Anne30]

I was diagnosed all at once in March. I cried for ages. I’m on Anastrozole and Ibrance. I’ve had two PET scans and both show good results. I’m working full time and apart from low white cell count haven’t yet experienced any side effects. It’s not always easy but for me it’s doable so far! Hope this is encouraging and sorry you are feeling the way you do. I remember it well x

[angiepops]

 Hi

I've been diagnosed with bone mets last week, 5 years after primary. Getting anastrozole and zoledronic acid infusions, is anyone else on this?

I keep crying a lot as well, not sure if its shock or the anastrozole. 

Angie

[riversidedawn]

Welcome Gill

Sorry you find yourself back here. I don't post often but read regularly and fine these ladies hugely supportive and open with their experiences.

I saw oncologist for scan results yesterday, pelvic tumours remain stable but there is activity in my T12 vertebra tumour. He said it's minor activity and only picked up because the scan I had is very powerful and would not have been picked up on other scans.

I've been on letrozole, ibrance, zometa and triptorelin since January. Oncologist says this could be an indication that the drugs are stopping working.

He's going to switch zometa to denosumab and apply for the cyberknife trial - there's a 50% chance that I get cyberknife instead of regular radiotherapy.

It's worry that the drugs are less effective already as trials indicated they could protect me for up to 2 years.

Gill which of your cocktail dp you put down to SEs as bad as chemo? I'm permanently fatigued and gave found my arthritis pain had worsened on my current regime. What's denosumab going to do to me?

Dies anyone else have experience of my new regime??

[gmc]

Hallo Ladies

My bone mets (and lung) were discovered in August this year after I broke a rib back in Dec and it wouldn't heal. Eventually a nuclear scan showed up the secondaries ! I had BC in 2002 and in the other breast in 2014 and am now devestated that this has now happened. My treatment for the last 3 months has been Denos umab injections, Exemestane and Everolimus which I've found nearly as tough as the chemo back in May 2014. I had a ct with contrast scan today and see the consultant next Tues for a comparison to see if the treatment is doing anything positive. I found the BCC forums really supportive before and although I never wanted to be back here it's a relief to read your threads and understand I'm not alone !

Cheers, Gill

[Flora29]

Thank you all, for your replies. And I’m so sorry you have these bone mets. 😞

I had my scan today, and have calmed down since I saw my consultant last week. I’ll forget it now, until next Monday when I get the results. My surgeon is really lovely, and said that when someone who doesn’t usually complain mentions something, they act. I didn’t go to my GP - I went straight to the BC Nurses at the hospital.

Keeping everything crossed xxx

[dragoncarine]

My bone mets were found accidentally after another unrelated procedure. You are so lucky you're getting scanned. I had gone to doctors severat times complaining of various pains but at no point did anyone suggest it might have anything to do with the breast cancer I had years ago. My pains are quite sharp - like being stabbed repeatedly rather than dull aches. 

[riversidedawn]

Hi Flora
I was diagnosed with primary in September 2014, 7cm and 2cm tumours with 26 lymph nodes affected.

When I was in hospital in September 2017 for diep reconstruction I had a CT scan because of breathing difficulties, lungs were clear but when my oncologist reviewed the scans 2 months later he spotted bone mets. Why he wasn't shown the scan in September I don't know! The bone mets had probably been there a while.

Hope your scan results are good news x

[bonariensis]

Hi Flora,
I didn't know I had bone mets when I had a CT scan investigating gut problems. There was no prob there but mets in my pelvis were picked up. A breast care surgeon had previously told me I was 'cured'.
It's good that your onc is sending you for a scan so promptly. Not knowing is the worst of all. I hope your results show no problems.
Hugs Bon x

[nicky08]

Hi Flora

Some ladies have not known they have got bone mets, I was one of them.  A routine mammogram showed a local recurrence then a subsequent bone scan picked up a couple of mets in my spine.  I now have quite extensive bone mets but that was because I was doing so well a few years back that my regular scans got spread out too much so the changes weren't spotted as quickly as they should have been.  On that occasion I did have a ache in my thigh which felt more muscular than anything but it turned out to be more bone mets.  Some ladies have had a spontaneous fracture, others have reported having aches which were then checked with scans.  It's not always obvious and unfortunately some GPs dismiss a lot of our concerns whereas they should take them seriously especially where there is a history of BC.

I hope your scans do give you the answers you need and that it isnt bone mets.  However you have found the right place to come should you need further support.

Nicky x

[Pippin]

Hi Flora

You may get many different replies to your question, but they are slow coming in. I limped a bit but have limped a long time since an old injury. After the first primary it was assumed to be the tamoxifen. At the second primary I had a CT scan and bone mets were diagnosed then and apparently were from the first primary. 

Your scan will hopefully be reassurring.

Pippin

[LYNDYLOO]

Hi everyone

Just thought I would join in regarding the discussion about treatments. The oncologist at the hospital I attend try to get the most out of each treatment so it is more a wait and see approach. Yes there are quite treatments for us but we might run out of options. That is what I was told anyway.

Linda

[Flora29]

Not sure I’m quite in the right section, but I am wondering how those with bone mets discovered they had them?

I’ve just been back to clinic today after I called my BC nurses and mentioned I had a tender spot on my collarbone. I will be getting a bone scan in the next week or so, back to see consultant in 2 weeks.

I had an MX and full lymph removal 9 years ago. And a WLE on my other boob 1 year ago.

Not sure if I am just being paranoid and over sensitive and whether to worry or be reassured that consultant has referred me straight through without question.

So, am curious about how you found yours?

[Lynnq]

Hello everyone

I was diagnosed with bone mets almost 6 years ago just 7 weeks after my primary diagnosis.  Also had shadows in my peritoneum .  I went onto Letrozole and Zometa which kept me stable for about 5 years then my TMs started to increase - scans showed more obvious infiltration in the peritoneum but my last scan also showed some differences in my lower back and the Onc told me that he suspected infiltration in my bone marrow.

I was put on cape and have just started my third cycle and my blood results have been very encouraging.  I didn’t ask much about the bone marrow suspicions and am wondering if anyone here has any experience of this....or can point me to a site that has some information.

I am finding that I have lower back pain and am wondering if that is the cause.  Have an appt with my GP next week to ask about pain killers.

xx

[ramade]

Mrs timps, sorry you've had to join us but you will find this forum amazing. i can only tell you that when my scans are looked at and there is any progression at all my treatment is changed. Do you have a sympathetic gp or a breast nurse you can talk to?

big hugs

Ramade

[funnyface]

Mrstimps, Some drs are more aggressive than others. They also go by how you feel. My oncologist will go and look at the scans herself if she isn't sure. If you aren't comfortable with this maybe a second opinion would be good. FF

[Mrstimps]

Hi Ladies,
Myself and my mom read the forum alot, shes not confident on posting so i said i would for her. She has mets in her lungs and bones, been on letrozole for the last 2.5 years and her latest scan has shown some progression. What we cant get out heads round is her consultant isnt changing her treatment yet and scanning her again in 3 months. Has anyone else experienced this? We aren’t sure wether to push for another opinion or trust that the docs know what they are doing, any advice appreciated x

[ramade]

Hi Linda so pleased for you that is great news. last time we talked we had both started on e/e,didn't work for me but glad you had a fair time with it. i imagine taxol is chemo, i recognise the name as a heavy 6 month dose years ago after my primary.Hope things keep going in the right direction for you.

love and hugs

Ramade x

[rosie53]

Yeyy fantastic news Linda!
Hugs Janette xx

[bonariensis]

Brilliant news Linda, so pleased for you.
Bon x

[funnyface]

That's great news Linda! Very excited for you. Go celebrate! FF

[LeighL]

Following a meeting wth the surgeon yesterday, it now seems that she would definitely like to do surgery in the New Year! Am currently gettng herceptin injections which are working very well, but she doesn't want to leave me undefended should I need to stop the herceptin for any reason. Surgeon and oncologist seem to have different opinions

[JWD]

Great news Linda.🤗🤗

[nicky08]

Wonderful news Linda. It makes the harsh SEs we have to put up with whilst on chemo all the more worth it doesn’t it? Thanks for sharing.

Nicky xx

[LYNDYLOO]

Hi everyone

Just thought I would post on the bone mets to let you know all know. Hospital rang yesterday regarding CT scan results. Liver tumour disappeared and bone is showing improvements. I am currently on weekly taxol. I have had 9 I down to havec12 in total.

I have not put much on here for a while with me being liver and bone mets now. Liver since last October.

Hope everyone is doing OK.

Linda

[LeighL]

Thanks Nicky. That's very useful and also reassuring. From a 6cm tumour it has shrunk to where it's barely detectable so the chemo and subsequent herceptin seem to be working extremely well. Have to speak to the surgeon today who will likely give me the same answer. Its been great to read so many positive posts on here!

[nicky08]

Hi Leigh

It is a lot to take in right now but we seem to learn and adjust along the way. In my own experience and after reading the experiences of many ladies on here over the years surgery is not given very often.

The reasoning behind this seems to be if you have a major operation, such as breast surgery, your immune system can be compromised which in turn can compromise your metastases. Most oncologists also like to have a reasonably time of stability, after initial treatment, to see how your particular BC, and SBC, reacts. If it is more aggressive they might not want to rock the boat so to speak. Their main aim is to prevent the mets spreading any further for as long as possible. By having chemo which will have been targeted to your type of BC it will have treated you systemically. Your original BC lump should have reacted to it as well. Also, from something that an oncologist said to me once, they can monitor the lump easier than bone mets etc which involve far more intrusive scans. My bone mets were found after a routine mammogram some 4-5 years after my primary. I had a local recurrence and was due a mastectomy but once the one mets were found it was straight into chemo nd then hormone treatments nd no surgery. I did ask over the years if I could have a biopsy or surgery and they said that on every CT scan I’d had there was no evidence of disease in the breast so it would have been pointless to have gone through surgery to have found nothing. By the way that was over 10 years ago and I’m still here! Over the years there’s been a lot of debate on this but there definitely doesn’t seem to be any pattern as to survival rates between those who didn’t have surgery for their primary (when they were diagnosed with secondaries at a similar time) to those that did, and very few (on the forum) have had the primary removed

Hope this helps or gives you some questions you may want to ask your oncologist.

Nicky x

[bonariensis]

Hi LeighL
I'm sorry you are having to join us. You're not stupid, there's such a lot to take in and you continue on a steep learning curve.
I don't have any experience of the question you are asking but if no-one else can help you I would talk to the BBC nurses who should be able to
Hugs Bon x

[LeighL]

Hi all, this is my first post so this is all new to me. Haven't read through all the posts and am a bit worried about sounding stupid! I was diagnosed in February and early on my oncologist had suspicions of a boney met in my sternum.  All along surgery had been discussed following initial chemotherapy.  However following chemotherapy there seems to be a turnaround where my onc. and the surgeon are both now thinking no surgery. Scans don't show any other secondaries bar the localised bone met. Any one else been in a similar situation and are wondering if it is best to get rid of the primary in the breast? Tks x

[ramade]

Good luck Bon, thinking of you today and thanks for the info you've put on line, interesting.

ramade x

[Annmat]

Hi Arem,

I’m sorry you find yourself here but we are all learning from each other n getting a lot of encouragement here. Take care and remember 1 step at a time.

[JWD]

Hello Arem
Sorry that you find yourself on here but welcome..I'm sure you will find lots of friendly advice from the ladies on here. I'm sure there will be someone posting on here soon to help you.xxx

[Arem]

i am new diagnosed with metastatic breast cancer with bone mets. i am er positive her positive.

[feelthefear]

Hi silver.
I’m doing well really. Apart from the pains which are not too bad, the flushes which are awful and the fatigue. 🙄
I get my first scan since starting treatment next month so will see if the side effects have been worth it.
I’m usually a sun seeker but have to admit I’m relieved the weather has cooled down. I’m sleeping much better without the unbearable heat.
It’s great that you have a pain consultant. I really hope they can help you. 🤞

Take care. Xxx

[riversidedawn]

Hello Ames, sorry you find yourself here at such a young age with young children. I'm 51 with 13 and 16 year olds.

I was diagnosed with spinal mets in January and started on zoladex, letrazol and palbociclib. My onc put me on all three at the same time (plus zometa bone strengthener injections) which was tough as I didn't know which was causing the side effects.

The regime is working well for me so far, scans in March and June showed reduction and stability respectively. I've got my next scan at the end of October.

I don't come on here very often but it's a lovely group of supportive ladies. Wishing you well with your treatment. Xxx

[riversidedawn]

RIP moijan. I've not been on for a while either so shocked when I just logged on. X

[ramade]

ff, absolutely! no options should get thrown out of the window. Different things work for different people simply because everybody responds differently, if this wasn't the case a cure would have been found. it is a highly complicated and very individual disease, well done, stay strong, 

love and hugs

Ramade xx

[funnyface]

Ramade, Thanks for that info on tamoxifen. I have never taken tamoxifen and talked to my oncologist about it. That as after ibrance and letrozole but before E & E. She told me since I had used a double agent that a single agent wouldn't work. That tamoxifen wasn't an option. I will be telling her no options get thrown out the window until I try them and they fail! My original oncologist threw all hormonals out til I pushed for them. He told me they would never work for me bc lupron injections did nothing as my first treatment. I've been on hormonal for 3 years now.  If my oncologist won't try tamoxifen, I will go elsewhere. 

I'm glad it's working for you. How long have you been doing metastatic BC now? I'm tired too. This year has been my worse for tiredness! 

Take care, FF

[silverlining]

Hello feel the fear,

I don't pop in here that often....how are you keeping? I really enjoy the autumn and I'm busy doing my X'mas shopping for family and friends.

You could not be more right about oncologists and pain. They should learn to be more supportive. Bad pain is bad pain. I've found myself a really decent Pain consultant and we are tinkering with my ongoing analgesia...

take eXtra special care of u.....xx..hugggs

[ramade]

Hi ff so glad to hear you are doing well, we really appreciate our granchildren as we have this darn cancer. e/e i started same time as you but didn't work unfortunately so i then had another 6 months of chemo, horrendous and didn't change a thing with the cancer so now i'm on tamoxifen which seems to be working, been on it 2 months, it makes me feel exhausted but i will just carry on with it and thankful that it makes me  better. i just keep making too much estrogen maybe. Anyway love to you and hope your scan brings continued good results in November

hugs Ramade

[funnyface]

Ramada, I'm OK. I've been  on E & E for 17 months. I'm still working PT. I have scan and check up in Nov. I hope I'm able to stay on this treatment longer. It messes with my diabetes and this is the most tired I have been, but I'm enjoying my granddaughter. Nov. will be the my 13 year mark of mets! 

How have you been doing? You have been at this awhile now too. I forget what treatment you are on. Wishing you the best! FF

[feelthefear]

It’s been a while since I visited the bone mets thread but just want to say it’s heartbreaking to hear about moijan. 😢 another one taken too soon.

Silver, sorry to hear you’re having a tough time at the moment. I really hope things improve for you soon. It seems that some oncologists think that as long as we’re still breathing then pain shouldn’t really matter to us. Xxx

[silverlining]

hello sammycat......x

[rah2321]

one of my relative is just diagonesed with MBC , originally it was discovered in 2005 ER+ pr - her-, grade II, now in 2018 she has been diagnosed as per ct scan + pet scan

1) bone mets 

2) general haziness of omental & mesentric 

Currently the medication is letrozole + ibrance + monthly injection

intially on songraphy mild ascites was deducted,

3) is general haziness is a definately indication the mets is in omental region or is it early stage

i can see you are having it since last 4 years, as on net it says the progonis is poor, currently what options we have and can it be change to chronic disease

Regards,